Novel phenotype and γ-glutamyl carboxylase mutations in combined deficiency of vitamin K-dependent coagulation factors

Haemophilia. 2011 Sep;17(5):822-4. doi: 10.1111/j.1365-2516.2011.02524.x. Epub 2011 Mar 24.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Carbon-Carbon Ligases / genetics*
  • Coagulation Protein Disorders / genetics*
  • DNA Mutational Analysis
  • Humans
  • Male
  • Mutation / genetics*
  • Phenotype
  • Vitamin K / metabolism
  • Vitamin K Deficiency / genetics*

Substances

  • Vitamin K
  • Carbon-Carbon Ligases
  • glutamyl carboxylase